5533-46-0

Usage

Uses

Used in Pharmaceutical Research:
1,3-dimethyl-2-selenourea is used as a potential therapeutic agent for its anti-cancer properties, targeting various types of cancer by modulating cellular processes and pathways that contribute to tumor growth and progression.
Used in Anti-inflammatory Applications:
1,3-dimethyl-2-selenourea is utilized as an anti-inflammatory agent, leveraging its capacity to reduce inflammation and alleviate symptoms associated with inflammatory conditions.
Used in Neurodegenerative Disease Treatment:
1,3-dimethyl-2-selenourea is being investigated for its potential use in treating neurodegenerative diseases, capitalizing on its ability to protect neurons and mitigate the effects of oxidative stress and inflammation that contribute to these conditions.
Used in Medicinal Chemistry:
1,3-dimethyl-2-selenourea serves as a valuable compound in medicinal chemistry for the development of new drugs and therapeutics, given its unique structural features and potential for modulating biological processes relevant to various diseases.

InChI:InChI=1/C3H7N2Se/c1-4-3(6)5-2/h1-2H3,(H,4,5)

Upstream product

• 96-31-1 N,N'-Dimethylurea 
• 4426-70-4 methyl isoselenocyanate 
• 74-89-5 methylamine 

Downstream Products

• 5533-47-1 3-methyl-2-methylimino-5-phenyl-selenazolidin-4-one 

Relevant academic research and scientific papers

COMPOUND FOR ORGANIC PHOTOELECTRIC DEVICE AND ORGANIC PHOTOELECTRIC DEVICE, IMAGE SENSOR AND ELECTRONIC DEVICE INCLUDING THE SAME

PROBLEM TO BE SOLVED: To provide a compound for an organic photoelectric device being capable of selectively absorbing light in a green wavelength region, and an organic photoelectric device, an image sensor and an electronic device include the same. SOLUTION: A compound for an organic photoelectric device is represented by Chemical Formula 1, where the definitions of substituents are as described in the specifications. SELECTED DRAWING: Figure 1 COPYRIGHT: (C)2017,JPOandINPIT

An experimental and theoretical approach to the study of the properties of parabanic acid and related compounds: Synthesis and crystal structure of diethylimidazolidine-2-selone-4,5-dione

The syntheses of the first examples of selenoparabanic acid derivatives (dialkylimidazolidine-2-selone-4,5-dione, 3eR, R = Me, Et, Bu) are presented along with the X-ray crystal structure determination of 3eEt. To gain an insight in the properties of parabanic acid derivatives on the basis of their electronic structures, we report the results of comparative hybrid-DFT calculations performed on parabanic, thioparabanic, and selenoparabanic acids (3aH, 3bH, and 3eH) and on their N,N′-dimethyl derivatives (3aMe, 3bMe, and 3eMe). Calculations show that the different nature of the frontier orbitals of 3aR compared to those of 3bR and 3eR, might account for the different reactivities of these compounds. Moreover, the weak donor character of 3bR and 3eR towards molecular di-iodine, estimated by FT-Raman measurements is in agreement with the calculated NBO-charge distribution.